{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1722","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1720","results":[{"created":"2020-07-21T23:00:02.721401+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DDX59 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DDX59","entity_type":"gene"},{"created":"2020-07-21T22:59:36.696650+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CSPP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CSPP1","entity_type":"gene"},{"created":"2020-07-21T22:59:12.086769+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CKAP2L was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CKAP2L","entity_type":"gene"},{"created":"2020-07-21T22:58:47.500355+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP41 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP41","entity_type":"gene"},{"created":"2020-07-21T22:58:21.965853+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP290 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-07-21T22:57:58.162760+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP164 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP164","entity_type":"gene"},{"created":"2020-07-21T22:57:34.253482+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP120 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP120","entity_type":"gene"},{"created":"2020-07-21T22:57:02.717726+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CENPF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CENPF","entity_type":"gene"},{"created":"2020-07-21T22:56:31.595997+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CCND2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CCND2","entity_type":"gene"},{"created":"2020-07-21T22:56:00.919859+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CC2D2A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CC2D2A","entity_type":"gene"},{"created":"2020-07-21T22:55:26.153865+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C5orf42 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C5orf42","entity_type":"gene"},{"created":"2020-07-21T22:55:01.646952+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C2CD3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C2CD3","entity_type":"gene"},{"created":"2020-07-21T22:54:34.116026+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BMP4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BMP4","entity_type":"gene"},{"created":"2020-07-21T22:54:07.555352+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BHLHA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BHLHA9","entity_type":"gene"},{"created":"2020-07-21T22:53:38.001493+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS9","entity_type":"gene"},{"created":"2020-07-21T22:52:05.502062+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS7","entity_type":"gene"},{"created":"2020-07-21T22:51:36.544563+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS5","entity_type":"gene"},{"created":"2020-07-21T22:51:07.888801+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS4","entity_type":"gene"},{"created":"2020-07-21T22:50:38.505190+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS2","entity_type":"gene"},{"created":"2020-07-21T22:50:09.284651+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS12","entity_type":"gene"},{"created":"2020-07-21T22:49:04.886570+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS10 as ready","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-07-21T22:49:04.876446+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs10 has been classified as Green List (High Evidence).","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-07-21T22:48:59.986059+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-07-21T22:48:36.205373+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS1 as ready","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-07-21T22:48:36.198661+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs1 has been classified as Green List (High Evidence).","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-07-21T22:48:33.481258+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS1 were changed from  to Bardet-Biedl syndrome 1, MIM#\t209900","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-07-21T22:47:49.636119+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-07-21T22:47:02.144602+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARL6 as ready","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-07-21T22:47:02.137244+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arl6 has been classified as Green List (High Evidence).","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-07-21T22:46:56.631111+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ARL6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-07-21T22:46:12.001228+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AKT3 as ready","entity_name":"AKT3","entity_type":"gene"},{"created":"2020-07-21T22:46:11.991549+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: akt3 has been classified as Green List (High Evidence).","entity_name":"AKT3","entity_type":"gene"},{"created":"2020-07-21T22:46:09.043388+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AKT3 were changed from  to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM#\t615937","entity_name":"AKT3","entity_type":"gene"},{"created":"2020-07-21T22:45:44.626142+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AKT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"AKT3","entity_type":"gene"},{"created":"2020-07-21T22:45:12.074194+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AHI1 as ready","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-07-21T22:45:12.065099+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ahi1 has been classified as Green List (High Evidence).","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-07-21T22:45:07.320663+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AHI1 were changed from  to Joubert syndrome 3, MIM#\t608629","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-07-21T22:44:22.924867+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AHI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-07-21T20:47:18.624268+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.367","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Deafness_ComplexAndIsolated to Deafness_IsolatedAndComplex","entity_name":null,"entity_type":null},{"created":"2020-07-21T20:45:44.978372+10:00","panel_name":"Deafness_ComplexAndIsolated","panel_id":209,"panel_version":"0.366","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Deafness to Deafness_ComplexAndIsolated","entity_name":null,"entity_type":null},{"created":"2020-07-21T14:26:15.183597+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: ALX3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALX3","entity_type":"gene"},{"created":"2020-07-21T14:25:55.761418+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: ALMS1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALMS1","entity_type":"gene"},{"created":"2020-07-21T14:25:29.642418+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: PDE6D: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-07-21T14:24:59.700123+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: CD96: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CD96","entity_type":"gene"},{"created":"2020-07-21T14:24:37.267758+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: ZSWIM6: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ZSWIM6","entity_type":"gene"},{"created":"2020-07-21T14:24:22.056400+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: ZNF141: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNF141","entity_type":"gene"},{"created":"2020-07-21T14:24:11.980284+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: WNT7A: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT7A","entity_type":"gene"},{"created":"2020-07-21T14:23:57.409495+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: WDR60: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR60","entity_type":"gene"},{"created":"2020-07-21T14:23:43.875988+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: WDR35: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR35","entity_type":"gene"},{"created":"2020-07-21T14:23:31.349642+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: WDR34: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR34","entity_type":"gene"},{"created":"2020-07-21T14:23:19.604620+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: WDR19: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR19","entity_type":"gene"},{"created":"2020-07-21T14:23:03.060503+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: WDPCP: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDPCP","entity_type":"gene"},{"created":"2020-07-21T14:22:37.747390+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: USP9X: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"USP9X","entity_type":"gene"},{"created":"2020-07-21T14:22:19.426954+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: UBE3B: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"UBE3B","entity_type":"gene"},{"created":"2020-07-21T14:22:03.626641+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TWIST1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TWIST1","entity_type":"gene"},{"created":"2020-07-21T14:21:45.838984+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TTC8: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2020-07-21T14:21:28.257620+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TTC21B: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TTC21B","entity_type":"gene"},{"created":"2020-07-21T14:21:08.295855+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TRAF3IP1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRAF3IP1","entity_type":"gene"},{"created":"2020-07-21T14:20:50.816623+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TMEM67: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM67","entity_type":"gene"},{"created":"2020-07-21T14:20:35.849007+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TMEM237: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM237","entity_type":"gene"},{"created":"2020-07-21T14:20:21.222152+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TMEM231: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM231","entity_type":"gene"},{"created":"2020-07-21T14:20:07.783960+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TMEM216: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM216","entity_type":"gene"},{"created":"2020-07-21T14:19:37.957533+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TMEM138: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM138","entity_type":"gene"},{"created":"2020-07-21T14:19:19.061933+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TFAP2B: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2020-07-21T14:19:02.107101+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TFAP2A: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2020-07-21T14:18:43.217497+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TCTN3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCTN3","entity_type":"gene"},{"created":"2020-07-21T14:18:30.432110+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TCTN2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCTN2","entity_type":"gene"},{"created":"2020-07-21T14:18:16.540321+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TCTEX1D2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCTEX1D2","entity_type":"gene"},{"created":"2020-07-21T14:18:00.422699+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TBX5: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX5","entity_type":"gene"},{"created":"2020-07-21T14:17:45.800352+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TBX3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX3","entity_type":"gene"},{"created":"2020-07-21T14:17:29.456156+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: TBX22: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"TBX22","entity_type":"gene"},{"created":"2020-07-21T13:31:29.440475+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: SPINT2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SPINT2","entity_type":"gene"},{"created":"2020-07-21T13:31:14.605997+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: SMOC1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-07-21T13:30:45.328530+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"edited their review of gene: SMO: Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SMO","entity_type":"gene"},{"created":"2020-07-21T13:30:08.828054+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: SMO: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMO","entity_type":"gene"},{"created":"2020-07-21T13:25:46.099837+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: SHH: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SHH","entity_type":"gene"},{"created":"2020-07-21T13:25:28.974958+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: SDCCAG8: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2020-07-21T13:25:06.422778+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: SC5D: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SC5D","entity_type":"gene"},{"created":"2020-07-21T13:24:53.224227+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: SALL4: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL4","entity_type":"gene"},{"created":"2020-07-21T13:24:39.648847+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: SALL1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL1","entity_type":"gene"},{"created":"2020-07-21T13:24:13.703623+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: RPGRIP1L: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2020-07-21T13:24:00.156275+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: RBM10: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RBM10","entity_type":"gene"},{"created":"2020-07-21T13:23:43.374016+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: RAB23: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB23","entity_type":"gene"},{"created":"2020-07-21T13:23:30.739396+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: PROM1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROM1","entity_type":"gene"},{"created":"2020-07-21T13:22:58.769214+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: PORCN: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"PORCN","entity_type":"gene"},{"created":"2020-07-21T13:22:26.820144+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: PNPLA6: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PNPLA6","entity_type":"gene"},{"created":"2020-07-21T13:22:01.170183+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: PITX1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PITX1","entity_type":"gene"},{"created":"2020-07-21T13:21:45.787131+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: PIK3R2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2020-07-21T13:21:20.637700+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: PIK3CA: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: Other","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2020-07-21T13:20:03.318371+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: OFD1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"OFD1","entity_type":"gene"},{"created":"2020-07-21T13:19:15.025566+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: NPHP3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NPHP3","entity_type":"gene"},{"created":"2020-07-21T13:19:01.258772+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: NEK1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NEK1","entity_type":"gene"},{"created":"2020-07-21T13:18:40.470208+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: MKS1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MKS1","entity_type":"gene"},{"created":"2020-07-21T13:18:25.488905+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: MKKS: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MKKS","entity_type":"gene"},{"created":"2020-07-21T13:18:10.692302+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: MEGF8: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MEGF8","entity_type":"gene"},{"created":"2020-07-21T13:17:47.725510+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: MBTPS2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"MBTPS2","entity_type":"gene"},{"created":"2020-07-21T13:17:28.634532+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: LZTFL1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2020-07-21T13:17:12.698101+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: LRP4: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T13:16:49.496287+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: LMBR1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LMBR1","entity_type":"gene"},{"created":"2020-07-21T13:16:29.981179+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.36","user_name":"Anand Vasudevan","item_type":"entity","text":"reviewed gene: LBR: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LBR","entity_type":"gene"}]}